ClinVar Miner

Submissions for variant NM_002473.5(MYH9):c.2205C>T (p.Asp735=) (rs370860479)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000242446 SCV000309034 likely benign not specified criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000402946 SCV000438434 likely benign Nonsyndromic Hearing Loss, Dominant 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000296989 SCV000438435 likely benign MYH9-related disorder 2016-06-14 criteria provided, single submitter clinical testing

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